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DYSGAMMAGLOBULINEMIA TYPE I

Annals of Internal Medicine, 1968
Excerpt To the Editor:I would like to disagree with a statement made by the authors of the paper entitled, "'Asymptomatic' Type I Dysgammaglobulinemia in Siblings" (Ann. Intern. Med.
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Thymic alymphoplasia and dysgammaglobulinemia type I

open access: closedThe Journal of Pediatrics, 1969
A.H. Greenberg, M. Ray, Y.T. Tsai
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[Analysis of dysgammaglobulinemia].

open access: closedRinsho byori. The Japanese journal of clinical pathology, 1972
K, Baba, T, Itoga
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Dysgammaglobulinemia in the Presence of Plasma Cells

New England Journal of Medicine, 1965
AS information about the gamma globulins has increased, it has become apparent that these are a heterogeneous group of proteins, varying in molecular size, antigenicity and electrophoretic mobility...
G J, GLEICH, J J, CONDEMI, J H, VAUGHAN
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HISTIOCYTIC REACTION IN DYSGAMMAGLOBULINEMIA AND CONGENITAL RUBELLA

Pediatrics, 1970
A girl was born of a mother who had rubella during the first trimester of pregnancy. The child showed failure to thrive, hepatosplenomegaly, lymphadenopathy, glaucoma, and nerve deafness. She also developed a dysgammaglobulinemia with low serum γM, low to absent γA, and high (19s) γM.
H N, Claman   +3 more
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THE GASTROINTESTINAL TRACT IN DYSGAMMAGLOBULINEMIA

open access: closed, 1969
MARVIN H. SLEISENGER, GRAHAM H. JEFFRIES
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Inherited Dysgammaglobulinemia of Chickens

1981
Disorders of the immune system leading to hypogammaglobulinemia are considered to be either primary defects in stem cell precursors of B lymphocytes or disorders in the maturation of B cells. In the X-linked form of immunodeficiency B cells are usually absent; however, patients with the form of immunodeficiency referred to as varied immunodeficiency ...
Albert A. Benedict   +2 more
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Type I dysgammaglobulinemia, systemic lupus erythematosus and lymphoma

The American Journal of Medicine, 1970
Abstract There is an increasing body of evidence based upon clinical reports and current concepts of immunopathogenesis that the association among connective tissue disease, immune deficiency and lymphoma is of considerable theoretic as well as practical importance.
C K, Smith, J T, Cassidy, G G, Bole
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Thymic alymphoplasia, previously reported as dysgammaglobulinemia type I

The Journal of Pediatrics, 1970
A child previously reported as having dysgammaglobulinemia type I was also demonstrated to have thymic alymphoplasia. His age and clinical course indicated that his disease was milder than the usual form. This may explain his earlier course, which was somewhat similar to that of Bruton's disease.
T M, Cashman, J J, Navin, S B, Chandor
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